birtwistle week2-lecture 2
DESCRIPTION
Deep mRNA sequensingTRANSCRIPT
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Experimental Methods in Systems Biology
Part of the Coursera Certificate in Systems Biology
Marc Birtwistle, PhDDepartment of Pharmacology & Systems TherapeuticsFall 2014, Week 2, Deep mRNA Sequencing
NIGMS funded Center
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2nd Generation Sequencing
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Sequencing by synthesis—2ndgeneration chemistry
Sequencing by synthesis can solve the issue of DNA strand separationafter addition of complimentary base
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Products of base addition reaction
Pyrophosphate
Hydrogen ion
dNTP
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Second (next) generation sequencing technologies
Company Platform Method Detection Length Advantages Disadvantages
Roche/454 FLX genome sequencer
PyrosequencingDetecion ofpyrophosphaterelease
Optical 0.4-1 Kb Long read length High cost; challengingsample prep.
Life Technologies IonPGMIonProton
Sequencing bysynthesis
Released H+ ions 200 bp Rapid runs, lowcost
Lower throughputcompared to Ilumina;Maturing technology
Illumina HiSeq 2500 MiSeq
Rev. terminatorsequencing bysynthesis
Fluorescence/ optical
2x150 or2x250 bp
Very high throughput
Long run time for standardruns
Life technologies 5500 SOLiD W system
Sequencing byligation
Fluorescence/ optical
1x75 or2x60 bp
Very high throughput
Short read lengths; non-standard data analysis
Illumina platform is market leader – one 30x coverage human genome for $5-10k
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Sequencing by synthesis:Detection and estimation of pyrophosphate release
454/Roche: First NGS sequencer in market
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Life/IonTorrent 'Electrical' Sequencing
● Polymerase releases H+ during base incorporation● Measured by semi‐conductor wafer● Essentially a massively parallel pH meter
Sequencing by detecting H+ release after addition of the base
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Dye sequencing by synthesis using reversible terminator
Grow
T
Measure
T
Reset
T
Grow
T
GX
X
X X
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Reversible dye chemistry
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Non‐Well format massively parallel sequencing by Illumina
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Limitations of second‐generation sequencing
● Second generation sequencing requires amplification to get sufficient number ofsequences to meet detection thresholds.
● Coverage of GC rich sequences● Amplification bias
● Inherently a problem for quantitation● Unique molecular identifiers however may solve this problem (Islam et al., Nat Methods, 2014;
Kivioja et al., Nat Methods, 2012)—see Week 1
● Second Gen Seq technologies have practical limits in read length● Mapping of long repeat regions in the genome● Identification and mapping of duplicate genes and pseudogenes
● Third‐generation sequencing seeks to therefore have longer read length without amplification
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Third‐generation sequencing technologies
Company Platform Method Detection Length Advantages Disadvantages
Pacific Biosciences
PacBio RS II Single-molecule real-time sequencing
Fluorescence/ optical
Up to 20Kb Very long read length
High per-base error rate and cost; low throughput
Oxford Nanopore
GridIONMinION
Nanopore sequencing
Voltage Sensing >10kb? Very long read lengths, Low cost and low error rates, fast run times?
???
PacBio is currently market leader
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PacBio real‐time sequencing
Pacific Biosciences RSImmobilized Polymerases + fluorescent dNTP +
really, really good optics
The particular polymerase used (“displacing”) is on the order of bp/sec
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Detection of base incorporation
Extension results in different fluorescent signal for each base
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Detecting base modifications